File:Autorecessive.svg
Size of this PNG preview of this SVG file: 512 × 599 pixels. Other resolutions: 205 × 240 pixels | 410 × 480 pixels | 656 × 768 pixels | 875 × 1,024 pixels | 1,750 × 2,048 pixels | 1,350 × 1,580 pixels.
Original file (SVG file, nominally 1,350 × 1,580 pixels, file size: 3 KB)
 | This is a file from the Wikimedia Commons. Information from its description page there is shown below. Commons is a freely licensed media file repository. You can help. |
 | This is a featured picture, which means that members of the community have identified it as one of the finest images on the English Wikipedia, adding significantly to its accompanying article. If you have a different image of similar quality, be sure to upload it using the proper free license tag, add it to a relevant article, and nominate it. |
 | This image was selected as picture of the day on the English Wikipedia for May 14, 2014. |
|
Summary
| Description |
English: Autosomal recessive gene Español: Gen autosómico recesivo. Modo de herencia entre dos portadores de un gen autosómico recesivo y monogénico. |
| Date | |
| Source | Own work in Inkscape |
| Author | en:User:Cburnett |
| Permission (Reusing this file) |
GFDL |
| Other versions |
[]
|
| SVG development |  This diagram was created with a text editor.  Please do not replace the simplified code of this file with a version created with Inkscape or any other vector graphics editor  |
Licensing
I, the copyright holder of this work, hereby publish it under the following licenses:
|
Permission is granted to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.2 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts. A copy of the license is included in the section entitled GNU Free Documentation License. |
  
|
This file is licensed under the Creative Commons Attribution-Share Alike 3.0 Unported license. | |
| ||
| This licensing tag was added to this file as part of the GFDL licensing update. |
You may select the license of your choice.
| Annotations | This image is annotated: View the annotations at Commons |
File history
Click on a date/time to view the file as it appeared at that time.
| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 18:06, 18 September 2023 | | 1,350 × 1,580 (3 KB) | Puck04 | remake (by hand); path text --> <text> |
| 01:14, 27 October 2019 |  | 1,350 × 1,580 (75 KB) | Reywas92 | Rm unnecessary scare quotes | |
| 18:01, 21 April 2007 |  | 1,350 × 1,580 (38 KB) | Cburnett | Enlarge "R" and "r" circles; combined caption of unaffected carriers into one. | |
| 12:51, 21 April 2007 |  | 1,350 × 1,580 (38 KB) | Lwollert | {{Information |Description={{en|Autosomal recessive gene inheritance}} |Source=en:User:Cburnett's work in Inkscape, minor alteration in inkscape |Date=April 21, 2007 |Author=en:User:Cburnett |Permission=G | |
| 19:26, 25 March 2007 |  | 1,350 × 1,580 (38 KB) | Cburnett | Fix arrows | |
| 19:18, 25 March 2007 |  | 1,350 × 1,580 (36 KB) | Cburnett | {{Information |Description={{en|Autosomal recessive gene}} |Source=Own work in Inkscape |Date=March 25, 2007 |Author=en:User:Cburnett |Permission=GFDL |other_versions= }} |
File usage
More than 100 pages use this file. The following list shows the first 100 pages that use this file only. A full list is available.
- 2-Hydroxyglutaric aciduria
- Abetalipoproteinemia
- Aceruloplasminemia
- Acheiropodia
- Acrodermatitis enteropathica
- Adducted thumb syndrome
- Adenine phosphoribosyltransferase deficiency
- Adenylosuccinate lyase deficiency
- Alpha-mannosidosis
- Apparent mineralocorticoid excess syndrome
- Ataxia–telangiectasia
- Atelosteogenesis, type II
- Batten disease
- Behr syndrome
- Berdon syndrome
- Beta-ketothiolase deficiency
- Biotinidase deficiency
- Bloom syndrome
- Blue diaper syndrome
- Canavan disease
- Carnitine-acylcarnitine translocase deficiency
- Carnitine palmitoyltransferase II deficiency
- Carnitine palmitoyltransferase I deficiency
- Carpenter syndrome
- Cartilage–hair hypoplasia
- Chondrodystrophy
- Cockayne syndrome
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Craniodiaphyseal dysplasia
- Cystic fibrosis
- Cystinosis
- Diastrophic dysplasia
- Dubin–Johnson syndrome
- Familial Mediterranean fever
- Familial dysautonomia
- Fanconi anemia
- Fountain syndrome
- Fraser syndrome
- Friedreich's ataxia
- Fumarase deficiency
- GM2-gangliosidosis, AB variant
- Giant axonal neuropathy
- Gitelman syndrome
- Glutaric acidemia type 2
- Glycine encephalopathy
- Glycogen storage disease type I
- Glycogen storage disease type II
- Glycogen storage disease type III
- Griscelli syndrome
- Hartnup disease
- Histidinemia
- Holocarboxylase synthetase deficiency
- Human genetics
- Hurler syndrome
- Isovaleric acidemia
- Jervell and Lange-Nielsen syndrome
- Lafora disease
- Leukodystrophy
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- Lucey–Driscoll syndrome
- Lysinuric protein intolerance
- Meleda disease
- Methemoglobinemia
- Methylmalonic acidemias
- Mitochondrial trifunctional protein deficiency
- Mucolipidosis
- Mucolipidosis type IV
- Mucopolysaccharidosis
- N-Acetylglutamate synthase deficiency
- Omenn syndrome
- Otospondylomegaepiphyseal dysplasia
- Pendred syndrome
- Persistent Müllerian duct syndrome
- Phenylketonuria
- Progressive familial intrahepatic cholestasis
- Propionic acidemia
- Pseudoxanthoma elasticum
- Robinow syndrome
- Situs inversus
- Sly syndrome
- Spinocerebellar ataxia
- Succinic semialdehyde dehydrogenase deficiency
- Sugarman syndrome
- Tangier disease
- Tay–Sachs disease
- Tetrahydrobiopterin deficiency
- Thalassemia
- Trimethylaminuria
- Tyrosinemia
- Very long-chain acyl-coenzyme A dehydrogenase deficiency
- Von Willebrand disease
- Walker–Warburg syndrome
- Weissenbacher–Zweymüller syndrome
- Werner syndrome
- Wilson's disease
- Wolfram syndrome
- Xeroderma pigmentosum
- ZAP70 deficiency
- Talk:Dominance (genetics)
View more links to this file.
Global file usage
The following other wikis use this file:
- Usage on ar.wikipedia.org
- Usage on bg.wikipedia.org
- Usage on bn.wikipedia.org
- Usage on bs.wikipedia.org
- Genetika čovjeka
- Perzistentni sindrom Müllerovog kanala
- Metahromatska leukodistrofija
- Methemoglobinemija
- Nedostatak holokarboksilazne sintetaze
- Jervellov i Lange-Nielsenov sindrom
- Sindrom arterijske vijugavosti
- Donohueov sindrom
- Bolest s mokraćom mirisa javorovog sirupa
- Cistična fibroza
- Cistinoza
- Bolest skladištenja glikogena tipa II
- Canavanova bolest
- Mukopolisaharidoza
- Nedostatak acil-koenzima dugolančane A dehidrogenaze
- Battenova bolest
- Porodična mediteranska groznica
- Talasemija
- Tirozinemija
- Ravna rožnjača
- Trimetilaminurija
- Nedostatak karnitin-palmitoiltransferaze II
- Tay-Sachsova bolest
- Bloomov sindrom
- Nedostatak 3-hidroksiacil-koenzima dugolančane dehidrogenaze A
- Nedostatak mitohondrijskog trifunkcionalnog proteina
- Atransferinemija
- Nedostatak biotinidaze
- Nedostatak karnitin-acilkarnitin translokaze
- Seckelov sindrom
- Propionska acidemija
- Xeroderma pigmentosum
- Wolframov sindrom
- Muenkeov sindrom
- Metilmalonska acidemija
- Nedostatak tetrahidrobiopterina
- Ahondrogeneza tip 1B
- Atelosteogeneza tip II
- AB varijanta GM2-gangliozidoze
- Cockayneov sindrom
- Diastrofijska displazija
- Sandhoffova bolest
- Nethertonov sindrom
View more global usage of this file.
